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6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride → 2-[[6-Fluoro-2-(4-fluorophenyl)quinazolin-4-yl]carbonyl]-6-methoxy-1,2,3,4-tetrahydroisoquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 2920335 | — |
| 反応物 | 6-Fluoro-2-(4-fluorophenyl)quinazoline-4-carboxylic acid | HCID 90410713 | — |
| 生成物 | 2-[[6-Fluoro-2-(4-fluorophenyl)quinazolin-4-yl]carbonyl]-6-methoxy-1,2,3,4-tetrahydroisoquinoline | HCID 86267783 | 50.6% |
反応手順
Reaction of 6-fluoro-2-(4-fluorophenyl)quinazoline-4-carboxylic acid with 6-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride gave compound 99 (50.6% yield). 1H NMR (400 MHz, DMSO-d6) δ 2.80 and 3.03 (2t, 2H), 3.54 and 4.02 (2t, 2H), 3.72 and 3.74 (2s, 3H), 4.47 and 4.92 (2s, 2H), 6.65-7.27 (m, 3H), 7.40-7.48 (m, 1H), 7.62-7.82 (m, 2H), 8.05-8.10 (m, 1H), 8.20-8.39 (m, 3H); MS (ESI) m/z 432 ([M+H]+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09193707B2 |
| 出典データセット | uspto-grants-2015_11 |
| ORD ID | ord-357ccab4ac54465c96c852c671547cbd |
| 出典メモ | uspto-grants-2015_11 |